For researchers

Is your paper here?

2,676 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

27 matches for Laisk T, showing the first 20.

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs12187932 rs61208973 rs568849616 rs76181804 rs9290877 rs9594366
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs11892008 rs6151589 rs4713343 rs2485662 rs78416326 rs17804499
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
rs146420876 rs10221244 rs76568468 rs9310423 rs10740388 rs34696920
Uncovering the shared genetic components of thyroid disorders and reproductive health
Estonian Biobank Research Team · Health Informatics Research Team
European journal of endocrinology · 2024 · PMID 39067062
12 pages+
rs1790604 rs2288188 rs9494311 rs71581958 rs1516960 rs4078470
Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses
Estonian Biobank Research Team
Nature medicine · 2025 · PMID 40069456
12 pages+
rs12475639 rs71648550 rs1239681 rs1935050 rs67679138 rs11123172
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Genes & Health Research Team · Estonian Biobank Research Team and 3 more consortia
Nature genetics · 2025 · PMID 40229599 · open access
12 pages+
rs17803970 rs10997841 rs10929759 rs3730074 rs7300155 rs2319754
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
rs1635501 rs10183486 rs2153157 rs12294104 rs10852344 rs12461110
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
rs2021095 rs6733156 rs4148211 rs2788095 rs4805129 rs58238559
Identifying Atopic Dermatitis Risk Loci in 1,094,060 Individuals with Subanalysis of Disease Severity and Onset
FinnGen · Estonian Biobank Research Team
The Journal of investigative dermatology · 2024 · PMID 38663478
7 pages
rs933905994 rs7481797 rs763581386 rs6064053 rs538763482 rs13275449
A large-scale genome-wide association study on female genital tract polyps highlights role of DNA repair, cell proliferation, and cell growth
Estonian Biobank Research Team
Human reproduction (Oxford, England) · 2025 · PMID 39986329
6 pages
rs13069734 rs16860234 rs72765685 rs79342925 rs9324897 Female Genital Tract Polyps
Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome
FinnGen Consortium, Estonian Biobank Research Team
Human reproduction (Oxford, England) · 2022 · PMID 34791234 · open access
5 pages
rs7564590 rs3945628 rs1672716 rs11031002 rs145598156
Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis
Estonian Biobank Research Team
Gastroenterology · 2023 · PMID 36736436
5 pages
rs148849032 rs66491909 rs12688091 rs12689287 Acute Pancreatitis
Hirsutism beyond PCOS: Genome-wide evidence for genetic factors
FinnGen · Estonian Biobank Research Team
The Journal of investigative dermatology · 2026 · PMID 42190866
5 pages
rs150735020 rs199649605 rs180731645 rs544265360 Hirsutism
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
5 pages
rs72964564 rs77864822 rs7933420 rs10036439 rs613937
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
23andMe Research Team
PLoS genetics · 2018 · PMID 30566500 · open access
4 pages
rs9696009 rs1784692 rs1795379 rs8043701
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer
Estonian Biobank Research Team; FinnGen
Human molecular genetics · 2023 · PMID 36929174 · open access
4 pages
rs36214159 rs27069 rs12603332 rs35508382
Genetic effects on the timing of parturition and links to fetal birth weight
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
rs113828443 rs34555419 rs6472846 rs28654158
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis
FinnGen · Estonian Biobank Research Team
The Journal of allergy and clinical immunology · 2022 · PMID 34454985
3 pages
rs7666843 rs3862469 rs11786685
Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse
Estonian Biobank Research Team
Nature communications · 2022 · PMID 35739095 · open access
3 pages
rs12325192 rs201194999 Pelvic Organ Prolapse
Polygenic prediction of preeclampsia and gestational hypertension
Nature medicine · 2023 · PMID 37248299
2 pages
rs7318880 rs260017

Showing 20 of 27 · page 1 of 2

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.